NDC 71217-0063-01 - Intensive treatment bodycream for mommy to be and all skin
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 71217-0063
- Requested NDC
- 71217-0063-01
- Package NDCs from labels
- 71217-0063-1, 71217-0063-01
- Manufacturer
- inthismorning co ltd | cosmax inc
- Effective date
- 2023-06-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| citronellol, geraniol, linalool, limonene - inthismorning co ltd | cosmax inc | inthismorning co ltd | cosmax inc | 2023-06-15 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71217-0063-1 | Intensive treatment bodycream for mommy to be and all skin | 200 mL in 1 TUBE | CREAM | 200 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71217-0063 | INTENSIVE TREATMENT BODYCREAM FOR MOMMY TO BE AND ALL SKIN (CITRONELLOL, GERANIOL, LINALOOL, LIMONENE) CREAM [INTHISMORNING CO LTD] | 2 | Current NDC, 1 package rows | 20230616_f388310c-dfd9-b9b5-e053-2a95a90ab22d.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Hydrating extra concentrate serum | CITRONELLOL | inthismorning co ltd | f241bb23-9124-32fe-e053-2995a90a3437 | 2023-01-29 | Warnings | P01OUT964K |
| Hydrating luxurious roseoil | CITRONELLOL, GERANIOL | inthismorning co ltd | f3731f7e-df0f-d0a7-e053-2a95a90aee60 | 2023-01-29 | Warnings | P01OUT964K L837108USY |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.